AVL9 | |||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||
Aliases | AVL9 , KIAA0241, AVL9 cell migration associated | ||||||||||||||||||||||||
External IDs | OMIM: 612927 MGI: 1926187 HomoloGene: 62425 GeneCards: AVL9 | ||||||||||||||||||||||||
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Orthologs | |||||||||||||||||||||||||
Species | Human | Mouse | |||||||||||||||||||||||
Entrez | |||||||||||||||||||||||||
Ensembl | |||||||||||||||||||||||||
UniProt | |||||||||||||||||||||||||
RefSeq (mRNA) | |||||||||||||||||||||||||
RefSeq (protein) | |||||||||||||||||||||||||
Location (UCSC) | Chr 7: 32.5 – 32.59 Mb | Chr 6: 56.69 – 56.74 Mb | |||||||||||||||||||||||
PubMed search | [3] | [4] | |||||||||||||||||||||||
Wikidata | |||||||||||||||||||||||||
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AVL9 cell migration associated is a protein that in humans is encoded by the AVL9 gene. [5]
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Epigen also known as epithelial mitogen is a protein that in humans is encoded by the EPGN gene.
AT-rich interactive domain-containing protein 3B is a protein that in humans is encoded by the ARID3B gene.
Mucin 3A is a protein that in humans is encoded by the MUC3A gene.
Transcription factor LBX1 is a protein that in humans is encoded by the LBX1 gene.
KRT71 is a keratin gene. Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene encodes a protein that is expressed in the inner root sheath of hair follicles. The type II keratins are clustered in a region of chromosome 12q13.(provided by RefSeq, Jun 2009)
Neurofilament, heavy polypeptide (NEFH) is a protein that in humans is encoded by the NEFH gene.
Dynein axonemal light chain 1, (LC1) is a protein that in humans is encoded by the DNAL1 gene.
Gap junction delta-4 protein (GJD4), also known as connexin-40.1 (Cx40.1), is a protein that in humans is encoded by the GJD4 gene.
Gap junction beta-5 protein (GJB5), also known as connexin-31.1 (Cx31.1), is a protein that in humans is encoded by the GJB5 gene.
The KSR2 gene is Kinase suppressor of ras 2 it is a protein that in humans is encoded by the KSR2 gene. KSR2 mutation effects in humans by obesity and because KSR2 gene reduces the ERK signaling and it reduces glucose and fatty acid oxidation. KSR2 mutation reduces the glucose and fatty acid oxidation process but it makes growth factor "Epidermal growth factor (EGF)" reaction more faster to simulate cell growth and KSR2 cause insulin resistance, KSA2 gene also regulates how the body uses the energy, and it usually causes type 2 diabetes.
Leishmanolysin-like is a protein that in humans is encoded by the LMLN gene.
Germ cell-less, spermatogenesis associated 1 is a protein that in humans is encoded by the GMCL1 gene.
Insulin like 6 is a protein that in humans is encoded by the INSL6 gene.
Forkhead box Q1 is a protein that in humans is encoded by the FOXQ1 gene.
Solute carrier family 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene.
Shroom family member 2 is a protein that in humans is encoded by the SHROOM2 gene.
Transmembrane protein 243 is a protein that in humans is encoded by the TMEM243 gene.
Stimulator of chondrogenesis 1 is a protein that in humans is encoded by the SCRG1 gene.
Tetraspanin 14 is a protein that in humans is encoded by the TSPAN14 gene.